Certain New Chemicals; Receipt and Status Information for January 2019; Correction, 25041-25042 [2019-11260]
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Federal Register / Vol. 84, No. 104 / Thursday, May 30, 2019 / Notices
extending into their LEPC’s jurisdiction.
Individuals anywhere may use the
Vulnerable Zone Indicator System
(VZIS) to find out whether a specified
address is within the vulnerable zone of
one or more stationary sources.
The final rule also authorizes and
encourages state and local government
officials to have access to OCA
information relevant to their
jurisdiction, both for their own official
use and to appropriately disseminate to
the local public population.
This ICR is intended to renew EPA’s
approval to carry out the recordkeeping
and reporting requirements crated by
the final rule as it defines the practices
that state and local officials need to
follow in order to share the data they
have and the specific procedures that
different categories of individuals need
to follow in order to request
information, certify their identity, and
receive OCA data.
Form Numbers: None.
Respondents/affected entities: State
and local agencies and the public.
Respondent’s obligation to respond:
Required to obtain or retain a benefit (40
CFR 1400).
Estimated number of respondents:
315 (total).
Frequency of response: As necessary.
Total estimated burden: 367 hours
(per year). Burden is defined at 5 CFR
1320.03(b).
Total estimated cost: $16,252 (per
year), includes $23 annualized capital
or operation & maintenance costs.
Changes in the Estimates: This ICR
renewal includes a significant decrease
in the estimated burden compared to the
previous ICR renewal. The burden
reduction is attributable to the reduced
number of reading room visits by the
public, the reduced number of letters of
request for OCA from state and local
governments and LEPCs, and a reduced
number of public meetings assumed to
be held by LEPCs resulting from the
lower of letters of request submitted by
LEPCs. To a large extent, the reductions
are the result of the respondents
increasingly obtaining the OCA data
through electronic methods, for
example, through rtk.net, RMP*Info and
RMP Data Download.
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2019–11271 Filed 5–29–19; 8:45 am]
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ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2019–0075; FRL–9994–01]
Certain New Chemicals; Receipt and
Status Information for January 2019;
Correction
Environmental Protection
Agency (EPA).
ACTION: Notice; correction.
AGENCY:
EPA is hereby correcting
information presented in a notice that
published in the Federal Register of
April 10, 2019. That notice provided
information concerning submissions to
EPA under TSCA Section 5, but
inadvertently duplicated test
submission information from the
previous month. EPA is providing the
test information received in January
2019, and providing an opportunity for
public comment on this information.
DATES: Comments identified by the
specific case number provided in this
document must be received on or before
July 1, 2019.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2019–0075,
and the specific case number for the
chemical substance related to your
comment, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute.
• Mail: Document Control Office
(7407M), Office of Pollution Prevention
and Toxics (OPPT), Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Jim
Rahai, Information Management
SUMMARY:
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25041
Division (7407M), Office of Pollution
Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
telephone number: (202) 564–8593;
email address: rahai.jim@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCA-Hotline@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. What action is the Agency taking?
In the Federal Register of April 10,
2019 (84 FR 14365) (FRL–9991–20),
EPA published information pertaining
to submissions in January 2019 under
TSCA Section 5, including notice of
receipt of a Premanufacture notice
(PMN), Significant New Use Notice
(SNUN) or Microbial Commercial
Activity Notice (MCAN), including an
amended notice or test information; an
exemption application (Biotech
exemption); an application for a test
marketing exemption (TME), both
pending and/or concluded; a notice of
commencement (NOC) of manufacture
(including import) for new chemical
substances; and a periodic status report
on new chemical substances that are
currently under EPA review or have
recently concluded review. Subsequent
to that publication, a stakeholder
noticed that the information in Table II
of Unit III. appeared to be identical to
the information provided for December
2018 (see 84 FR 14368, April 10, 2019)
(FRL–9990–59). EPA is hereby
publishing the corrected information for
January 2019 and providing an
opportunity for public comments on
this new information.
II. What is this correction?
In Unit I.A., the first sentence
incorrectly identified the period covered
by the notice as ‘‘from 01/01/2019 to 12/
31/2019,’’ rather than just the month of
January. Instead, it should have
identified the period covered by the
notice as ‘‘from 01/01/2019 to 01/31/
2019.’’
In addition, the information in Table
II of Unit III., which appears on page
14367, is corrected to read as follows:
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Federal Register / Vol. 84, No. 104 / Thursday, May 30, 2019 / Notices
TABLE II—TEST INFORMATION RECEIVED FROM 01/01/2019 TO 01/31/2019
Case No.
Received date
P–11–0483 ....
1/3/2019
SN–18–0013 ..
P–19–0019 ....
1/3/2019
1/3/2019
P–16–0462 ....
1/9/2019
P–13–0679 ....
1/10/2019
P–19–0032 ....
1/15/2019
P–16–0150 ....
1/16/2019
P–16–0543 ....
P–10–0183 ....
1/18/2019
1/23/2019
P–10–0184 ....
1/23/2019
P–10–0185 ....
1/23/2019
P–10–0186 ....
1/23/2019
P–14–0712 ....
1/28/2019
Type of test information
Mouse and Rat Combined Repeated-Dose Oral (Gavage) Toxicity Study with the Reproduction/Developmental Toxicity Screening Test (OECD Test
Guideline 422).
Industrial Hygiene Monitoring Report ...........................
Skin Irritation Study; Reconstructed human Cornealike Epithelium (RhCE) test method for identifying
chemicals not requiring classification and labelling
for eye irritation or serious eye damage (OECD
Test Guideline 492).
Metals Analysis Report Quarter 4 2018 .......................
Routine/Annual/Quarterly Testing and Reporting: Certification of Analysis.
Test Item related to chemical composition, purity,
strength, stability and other data required by current
OECD Good Laboratory Practices (OECD Test
Guidelines 101–105, 109, 111, 117 and 121).
A 5-day Toxicity Study of HCFC–243db by WholeBody Inhalation in Sprague Dawley Rats, 5-day
Toxicity Study of HCFC–243db by Whole-Body Inhalation in CD–1 Mice, and 5-day Toxicity Study of
HCFC–243db by Whole-Body Inhalation in Albino
Rabbits.
Exposure Monitoring Report .........................................
Routine/Annual Testing and Reporting: Certifications
of Analysis.
Routine/Annual Testing and Reporting: Certifications
of Analysis.
Routine/Annual Testing and Reporting: Certifications
of Analysis.
Routine/Annual Testing and Reporting: Certifications
of Analysis.
PCCD/F EPA Test Method 8290A ...............................
As explained in the original notice,
(S) indicates that the information in the
table is the specific information
provided by the submitter, and (G)
indicates that this information in the
table is generic information because the
specific information provided by the
submitter was claimed as CBI.
Authority: 15 U.S.C. 2601 et seq.
Dated: May 23, 2019.
Megan Carroll,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2019–11260 Filed 5–29–19; 8:45 am]
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Chemical substance
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(G) Alkyl thiol.
(G) Lithiated metal oxide.
(G) Haloalkane.
(G) Ash (residues), reaction products
tetraethoxydioxa-polyheteroatom-disilaalkane.
(G) Fluoroalkyl acrylate copolymer.
(G) Carbonic dichloride, polymer with 4,4′-(1methylethylidene)bis[phenol] ester, polymer with
tetrol and polyether tetrol.
(G) Chlorofluorocarbon.
(G) Halogenophosphoric acid metal salt.
(G) Alkyl alkanoate.
(G) Alkyl ethoxylate.
(G) Alkyl phosphate salt.
(G) Alkyl phosphate salt.
(G) Waste plastics, pyrolyzed, C5–55 fraction.
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OECA–2011–0272; FRL–9994–
55–OMS]
Information Collection Request
Submitted to OMB for Review and
Approval; Comment Request;
Emission Guidelines for Hospital/
Medical/Infectious Waste Incinerators
(Renewal)
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Environmental Protection
Agency (EPA) has submitted an
information collection request (ICR),
Emission Guidelines for Hospital/
Medical/Infectious Waste Incinerators
(EPA ICR Number 1899.09, OMB
Control Number 2060–0422), to the
Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act. This is a proposed
extension of the ICR, which is currently
approved through May 31, 2019. Public
comments were previously requested,
via the Federal Register, on May 30,
2018 during a 60-day comment period.
SUMMARY:
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with
This notice allows for an additional 30
days for public comments. A fuller
description of the ICR is given below,
including its estimated burden and cost
to the public. An agency may neither
conduct nor sponsor, and a person is
not required to respond to, a collection
of information unless it displays a
currently valid OMB control number.
DATES: Additional comments may be
submitted on or before July 1, 2019.
ADDRESSES: Submit your comments,
referencing Docket ID Number EPA–
HQ–OECA–2011–0272, to: (1) EPA
online using www.regulations.gov (our
preferred method), or by email to
docket.oeca@epa.gov, or by mail to: EPA
Docket Center, Environmental
Protection Agency, Mail Code 28221T,
1200 Pennsylvania Ave. NW,
Washington, DC 20460; and (2) OMB via
email to oira_submission@omb.eop.gov.
Address comments to OMB Desk Officer
for EPA.
EPA’s policy is that all comments
received will be included in the public
docket without change, including any
personal information provided, unless
the comment includes profanity, threats,
information claimed to be Confidential
Business Information (CBI), or other
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Agencies
[Federal Register Volume 84, Number 104 (Thursday, May 30, 2019)]
[Notices]
[Pages 25041-25042]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-11260]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2019-0075; FRL-9994-01]
Certain New Chemicals; Receipt and Status Information for January
2019; Correction
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice; correction.
-----------------------------------------------------------------------
SUMMARY: EPA is hereby correcting information presented in a notice
that published in the Federal Register of April 10, 2019. That notice
provided information concerning submissions to EPA under TSCA Section
5, but inadvertently duplicated test submission information from the
previous month. EPA is providing the test information received in
January 2019, and providing an opportunity for public comment on this
information.
DATES: Comments identified by the specific case number provided in this
document must be received on or before July 1, 2019.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2019-0075, and the specific case number for the
chemical substance related to your comment, by one of the following
methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be Confidential Business
Information (CBI) or other information whose disclosure is restricted
by statute.
Mail: Document Control Office (7407M), Office of Pollution
Prevention and Toxics (OPPT), Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Jim Rahai, Information
Management Division (7407M), Office of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460-0001; telephone number: (202) 564-8593; email address:
[email protected].
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: [email protected].
SUPPLEMENTARY INFORMATION:
I. What action is the Agency taking?
In the Federal Register of April 10, 2019 (84 FR 14365) (FRL-9991-
20), EPA published information pertaining to submissions in January
2019 under TSCA Section 5, including notice of receipt of a
Premanufacture notice (PMN), Significant New Use Notice (SNUN) or
Microbial Commercial Activity Notice (MCAN), including an amended
notice or test information; an exemption application (Biotech
exemption); an application for a test marketing exemption (TME), both
pending and/or concluded; a notice of commencement (NOC) of manufacture
(including import) for new chemical substances; and a periodic status
report on new chemical substances that are currently under EPA review
or have recently concluded review. Subsequent to that publication, a
stakeholder noticed that the information in Table II of Unit III.
appeared to be identical to the information provided for December 2018
(see 84 FR 14368, April 10, 2019) (FRL-9990-59). EPA is hereby
publishing the corrected information for January 2019 and providing an
opportunity for public comments on this new information.
II. What is this correction?
In Unit I.A., the first sentence incorrectly identified the period
covered by the notice as ``from 01/01/2019 to 12/31/2019,'' rather than
just the month of January. Instead, it should have identified the
period covered by the notice as ``from 01/01/2019 to 01/31/2019.''
In addition, the information in Table II of Unit III., which
appears on page 14367, is corrected to read as follows:
[[Page 25042]]
Table II--Test Information Received From 01/01/2019 to 01/31/2019
----------------------------------------------------------------------------------------------------------------
Case No. Received date Type of test information Chemical substance
----------------------------------------------------------------------------------------------------------------
P-11-0483................... 1/3/2019 Mouse and Rat Combined Repeated- (G) Alkyl thiol.
Dose Oral (Gavage) Toxicity
Study with the Reproduction/
Developmental Toxicity
Screening Test (OECD Test
Guideline 422).
SN-18-0013.................. 1/3/2019 Industrial Hygiene Monitoring (G) Lithiated metal oxide.
Report.
P-19-0019................... 1/3/2019 Skin Irritation Study; (G) Haloalkane.
Reconstructed human Cornea-like
Epithelium (RhCE) test method
for identifying chemicals not
requiring classification and
labelling for eye irritation or
serious eye damage (OECD Test
Guideline 492).
P-16-0462................... 1/9/2019 Metals Analysis Report Quarter 4 (G) Ash (residues), reaction
2018. products with tetraethoxydioxa-
polyheteroatom-disilaalkane.
P-13-0679................... 1/10/2019 Routine/Annual/Quarterly Testing (G) Fluoroalkyl acrylate
and Reporting: Certification of copolymer.
Analysis.
P-19-0032................... 1/15/2019 Test Item related to chemical (G) Carbonic dichloride, polymer
composition, purity, strength, with 4,4'-(1-
stability and other data methylethylidene)bis[phenol]
required by current OECD Good ester, polymer with tetrol and
Laboratory Practices (OECD Test polyether tetrol.
Guidelines 101-105, 109, 111,
117 and 121).
P-16-0150................... 1/16/2019 A 5-day Toxicity Study of HCFC- (G) Chlorofluorocarbon.
243db by Whole-Body Inhalation
in Sprague Dawley Rats, 5-day
Toxicity Study of HCFC-243db by
Whole-Body Inhalation in CD-1
Mice, and 5-day Toxicity Study
of HCFC-243db by Whole-Body
Inhalation in Albino Rabbits.
P-16-0543................... 1/18/2019 Exposure Monitoring Report...... (G) Halogenophosphoric acid
metal salt.
P-10-0183................... 1/23/2019 Routine/Annual Testing and (G) Alkyl alkanoate.
Reporting: Certifications of
Analysis.
P-10-0184................... 1/23/2019 Routine/Annual Testing and (G) Alkyl ethoxylate.
Reporting: Certifications of
Analysis.
P-10-0185................... 1/23/2019 Routine/Annual Testing and (G) Alkyl phosphate salt.
Reporting: Certifications of
Analysis.
P-10-0186................... 1/23/2019 Routine/Annual Testing and (G) Alkyl phosphate salt.
Reporting: Certifications of
Analysis.
P-14-0712................... 1/28/2019 PCCD/F EPA Test Method 8290A.... (G) Waste plastics, pyrolyzed,
C5-55 fraction.
----------------------------------------------------------------------------------------------------------------
As explained in the original notice, (S) indicates that the
information in the table is the specific information provided by the
submitter, and (G) indicates that this information in the table is
generic information because the specific information provided by the
submitter was claimed as CBI.
Authority: 15 U.S.C. 2601 et seq.
Dated: May 23, 2019.
Megan Carroll,
Acting Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2019-11260 Filed 5-29-19; 8:45 am]
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